US20160103196A1 - Method and apparatus for magnetic resonance imaging - Google Patents

Method and apparatus for magnetic resonance imaging Download PDF

Info

Publication number
US20160103196A1
US20160103196A1 US14/882,793 US201514882793A US2016103196A1 US 20160103196 A1 US20160103196 A1 US 20160103196A1 US 201514882793 A US201514882793 A US 201514882793A US 2016103196 A1 US2016103196 A1 US 2016103196A1
Authority
US
United States
Prior art keywords
magnetic resonance
magnetic
gradient
refocusing
raw data
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US14/882,793
Other versions
US10267885B2 (en
Inventor
David Grodzki
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Siemens Healthineers AG
Original Assignee
Siemens AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Siemens AG filed Critical Siemens AG
Assigned to SIEMENS AKTIENGESELLSCHAFT reassignment SIEMENS AKTIENGESELLSCHAFT ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GRODZKI, DAVID
Publication of US20160103196A1 publication Critical patent/US20160103196A1/en
Application granted granted Critical
Publication of US10267885B2 publication Critical patent/US10267885B2/en
Assigned to SIEMENS HEALTHCARE GMBH reassignment SIEMENS HEALTHCARE GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SIEMENS AKTIENGESELLSCHAFT
Assigned to Siemens Healthineers Ag reassignment Siemens Healthineers Ag ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SIEMENS HEALTHCARE GMBH
Active legal-status Critical Current
Adjusted expiration legal-status Critical

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/44Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
    • G01R33/48NMR imaging systems
    • G01R33/54Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
    • G01R33/56Image enhancement or correction, e.g. subtraction or averaging techniques, e.g. improvement of signal-to-noise ratio and resolution
    • G01R33/565Correction of image distortions, e.g. due to magnetic field inhomogeneities
    • G01R33/56536Correction of image distortions, e.g. due to magnetic field inhomogeneities due to magnetic susceptibility variations
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/44Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
    • G01R33/48NMR imaging systems
    • G01R33/54Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
    • G01R33/56Image enhancement or correction, e.g. subtraction or averaging techniques, e.g. improvement of signal-to-noise ratio and resolution
    • G01R33/565Correction of image distortions, e.g. due to magnetic field inhomogeneities
    • G01R33/56563Correction of image distortions, e.g. due to magnetic field inhomogeneities caused by a distortion of the main magnetic field B0, e.g. temporal variation of the magnitude or spatial inhomogeneity of B0
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/44Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
    • G01R33/48NMR imaging systems
    • G01R33/54Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
    • G01R33/56Image enhancement or correction, e.g. subtraction or averaging techniques, e.g. improvement of signal-to-noise ratio and resolution
    • G01R33/565Correction of image distortions, e.g. due to magnetic field inhomogeneities
    • G01R33/56572Correction of image distortions, e.g. due to magnetic field inhomogeneities caused by a distortion of a gradient magnetic field, e.g. non-linearity of a gradient magnetic field
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/44Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
    • G01R33/48NMR imaging systems
    • G01R33/54Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
    • G01R33/56Image enhancement or correction, e.g. subtraction or averaging techniques, e.g. improvement of signal-to-noise ratio and resolution
    • G01R33/565Correction of image distortions, e.g. due to magnetic field inhomogeneities
    • G01R33/5659Correction of image distortions, e.g. due to magnetic field inhomogeneities caused by a distortion of the RF magnetic field, e.g. spatial inhomogeneities of the RF magnetic field
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/0017Means for compensating offset magnetic fields or the magnetic flux to be measured; Means for generating calibration magnetic fields
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/02Measuring direction or magnitude of magnetic fields or magnetic flux
    • G01R33/025Compensating stray fields
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/28Details of apparatus provided for in groups G01R33/44 - G01R33/64
    • G01R33/38Systems for generation, homogenisation or stabilisation of the main or gradient magnetic field
    • G01R33/387Compensation of inhomogeneities
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/28Details of apparatus provided for in groups G01R33/44 - G01R33/64
    • G01R33/38Systems for generation, homogenisation or stabilisation of the main or gradient magnetic field
    • G01R33/389Field stabilisation, e.g. by field measurements and control means or indirectly by current stabilisation

Definitions

  • the invention concerns a method for magnetic resonance imaging, a magnetic resonance apparatus and a computer-readable data storage medium.
  • a magnetic resonance apparatus also called a magnetic resonance tomography system
  • the body to be examined of an examination subject is conventionally exposed with the use of a basic field magnet to a relatively high basic magnetic field, for example of 1.5 or 3 or 7 tesla.
  • gradient switching operations occur with a gradient coil unit.
  • Radio-frequency pulses in particular excitation pulses, are then emitted by a radio-frequency antenna unit via suitable antennas, and this leads to the nuclear spins (spins) of specific atoms excited in a resonant manner by these radio-frequency pulses being tilted by a defined flip angle with respect to the magnetic field lines of the basic magnetic field.
  • radio-frequency signals known as magnetic resonance signals
  • the desired image data can be reconstructed from the raw data acquired in this way.
  • a specific magnetic resonance sequence also called a pulse sequence
  • a pulse sequence which includes a series of radio-frequency pulses, in particular radio-frequency excitation pulses, and gradient switching operations, which are activated in appropriate coordination with the radio-frequency pulses along different gradient axes in different spatial directions.
  • Readout windows that are appropriately timed are set, which specify the periods in which the induced magnetic resonance signals are detected.
  • An interference object may be present in an examination region of a magnetic resonance recording.
  • This interference object is characterized by having a magnetic susceptibility that differs from the magnetic susceptibility of tissue surrounding the interference object.
  • This interference object therefore can lead to magnetic interference fields that can make imaging of the interference object difficult and/or lead to image artifacts in the vicinity of the interference object.
  • An object of the invention is to enable improved magnetic resonance imaging in the vicinity of an interference object.
  • magnetic resonance raw data are acquired from the examination region by execution of a magnetic resonance sequence having multiple repetition intervals with refocusing of nuclear spins in the examination region at the end of each repetition interval, and wherein, during at least part of the duration of acquisition of the magnetic resonance raw data, a magnetic compensation gradient is activated that is opposed to the magnetic interference field.
  • the examination object can be a patient, a trainee or a phantom.
  • the examination region also called the field of view (FOV) is a volume of which an image is to be reconstructed from the acquired raw magnetic resonance data.
  • the reconstructed magnetic resonance image is presented, i.e. displayed on a display monitor for a user and/or stored in a database.
  • the raw data are compiled in a datafile in a memory during acquisition thereof, and the image data are also compiled in a datafile.
  • the interference object has a magnetic susceptibility that differs from the magnetic susceptibility of the material that surrounds the interference object.
  • the interference object in particular has a magnetic susceptibility that is different from the magnetic susceptibility of surrounding tissue of the examination object in the examination region.
  • the magnetic susceptibility of the interference object is higher than, often more than ten times higher than, the magnetic susceptibility of the material that surrounds the interference object.
  • the interference object can include metal.
  • the interference object can be, for example, a metallic implant in the examination object, such as an artificial hip joint.
  • the magnetic interference field of the interference object is produced due to the difference of the susceptibility of the interference object from the surrounding material.
  • the magnetic interference field can have a magnetic field gradient.
  • the magnetic interference field therefore can lead to at least one additional gradient moment being present during acquisition of the raw data.
  • the magnetic interference field of the interference object therefore can disrupt the nuclear spins that are excited during the magnetic resonance raw data acquisition.
  • the magnetic interference field typically disrupts a phase development and/or a phase position of the spins. This can mean that the excited spins are dephased due to the magnetic interference field, in particular drift apart. In this way the interference object can lead to a signal loss in the recorded magnetic resonance raw data in a vicinity of the interference object. In this way the magnetic interference field can disrupt refocusing of the spins.
  • the multiple repetition intervals in the magnetic resonance sequence will each have a duration of one repetition time.
  • the repetition time is typically defined as the duration that occurs between two radio-frequency excitation pulses of the magnetic resonance sequence.
  • the magnetic resonance sequence is advantageously designed as a single-shot magnetic resonance sequence. This means that the magnetic resonance raw data produce a number of magnetic resonance images.
  • raw data are acquired for reconstruction of one magnetic resonance image among the multiple magnetic resonance images.
  • the respective sets of raw data for the multiple magnetic resonance images are acquired consecutively, within a portion of each repetition time.
  • the spins can be refocused by a radio-frequency refocusing pulse.
  • the spins can be refocused by a refocusing gradient switching operation, also called refocusing gradient.
  • the refocusing gradient is switched in the phase encoding direction. Refocusing of the spins leads to a defined starting position (angle) of the spins at the beginning of a repetition interval. Refocusing of the spins conventionally involves refocusing dephased spins. Refocusing of the spins may also include a different change in the phase position of the spins.
  • the magnetic interference field of the interference object can disrupt this refocusing of the spins.
  • the compensation gradient in accordance with the invention is activated.
  • the magnetic compensation gradient is switched by the gradient coils that are conventionally present in the magnetic resonance scanner.
  • the compensation gradient is designed as a magnetic gradient field.
  • the compensation gradient is switched with the spatial encoding gradients in an overlaid manner, these spatial encoding gradients already being present in the magnetic resonance sequence.
  • the compensation gradient may also be switched in an overlaid manner on a refocusing gradient.
  • the compensation gradient is therefore switched (activated) in addition to the spatial encoding gradient and/or the refocusing gradient.
  • the fact that the magnetic compensation gradient is opposed to the magnetic interference field means that there is an increase in the magnetic compensation gradient in a direction that is opposite to the direction of increase in the magnetic interference field.
  • the gradient moment of the compensation gradient is also designed so as to be opposed to the gradient moment of the magnetic interference field.
  • the gradient moment is typically defined by the time integral of the amplitude of a gradient switching operation.
  • Interference to the refocusing of the spins due to the magnetic interference field can be at least partially prevented by the approach according to the invention.
  • the compensation gradient can ensure that the spins are more correctly refocused at the end of each repetition interval of the multiple repetition intervals.
  • the raw data for each magnetic resonance image among the multiple magnetic resonance images thus are acquired, in each repetition interval of the multiple repetition intervals, on a comparable basis and/or under standardized boundary conditions.
  • magnetic resonance imaging can be carried out particularly effectively in the vicinity of the interference object.
  • artifact-reduced magnetic resonance image data to be generated with the method according to the invention.
  • the tissue of the examination object can be correctly shown in the magnetic resonance image data.
  • a number of sets of magnetic resonance raw data from the examination region can be acquired in a number of magnetic resonance scans.
  • a different compensation gradient can then be switched during each raw data set acquisition to compensate a different magnetic interference field.
  • a first set of magnetic resonance raw data therefore can be acquired in a first magnetic resonance scan using a first compensation gradient that compensates a first magnetic interference field
  • a second set of magnetic resonance raw data can be acquired using a second compensation gradient that compensates a second magnetic interference field.
  • Different interference fields which are caused by one or more interference object(s) in the examination region, can thereby be particularly accurately compensated.
  • the magnetic compensation gradient is switched such that interference, caused by the magnetic interference field, to the refocusing of the spins in the examination region is at least partially compensated.
  • the gradient moment of the magnetic compensation gradient is chosen such that the gradient moment of the magnetic interference field is at least partially compensated. This can ensure extensive, possibly complete, refocusing of the spins in the examination region. The extensive, in particular complete, refocusing of the spins is then present at the beginning of each repetition interval of the multiple repetition intervals.
  • the compensation gradient is switched for the entire duration of acquisition of the magnetic resonance raw data.
  • the compensation gradient is then switched for the entire repetition interval. In this way a disruptive gradient moment of the magnetic interference field can be reliably compensated throughout the entire recording of the magnetic resonance image data.
  • the compensation gradient is switched during refocusing of the spins in the examination region at the end of each repetition interval of the multiple repetition intervals.
  • the compensation gradient is therefore advantageously switched only if refocusing of the spins occurs.
  • the compensation gradient is therefore advantageously activated in precisely that period during which refocusing of the spins occurs.
  • the compensation gradient is switched only at the end of each repetition interval. It is advantageous to switch the compensation gradient selectively during refocusing because a dephasing of spins, produced by the compensation gradient, which are not affected by the magnetic interference field, can therefore be at least partially prevented and/or reduced.
  • the compensation gradient thus can advantageously be matched to the requirements for refocusing of the spins.
  • refocusing of the spins in the examination region includes refocusing of a gradient-induced phase development of the spins in the examination region by a refocusing gradient, and the compensation gradient is switched during the refocusing gradient in addition to the refocusing gradient.
  • the refocusing gradient is switched in the phase encoding direction, so the gradient-induced phase development of the spins can be refocused.
  • the compensation gradient is then switched in addition to the refocusing gradient, so the interference in the phase development of the spins, caused by the interference object, can be at least partially compensated.
  • This approach is based on the concept that the refocusing gradient is typically fixed by the magnetic resonance sequence. The refocusing gradient therefore typically cannot be variably adjusted to the presence of the interference object in the examination region.
  • the compensation gradient can then advantageously take on this task.
  • the compensation gradient can modulate the refocusing gradient so an optimum refocusing of the spins in the examination region can be attained, while taking account of the magnetic interference field of the interference object.
  • the refocusing gradient and the compensation gradient are switched in an overlaid manner by the gradient coil, so an effective compensation-refocusing gradient switching operation is carried out at the end of each repetition interval of the multiple repetition intervals.
  • parameters of the compensation gradient are ascertained as a function of parameters of the refocusing gradient.
  • Parameters of a gradient switching operation can be, for example, the amplitude of the gradient switching operation, the duration of the gradient switching operation, the slew rate of the gradient switching operation, etc. Further parameters of the gradient switching operation that sre4 considered expedient by those skilled in the art are also conceivable.
  • the compensation gradient can be advantageously matched to the refocusing gradient by ascertaining the parameters of the compensation gradient as a function of the parameters of the refocusing gradient.
  • the spins in the examination region can be particularly effectively refocused in this way.
  • the magnetic resonance sequence is a steady-state free precession (SSFP) magnetic resonance sequence.
  • An SSFP magnetic resonance sequence typically includes a sequence of radio-frequency excitation pulses with the condition that the repetition time, i.e. the duration of a repetition interval, is less than the T 2 relaxation time of the relevant tissue of the examination object.
  • the radio-frequency excitation pulses are therefore switched in an interval, the repetition time, which is smaller than the T 2 time. Magnetization of the spins in the steady state can therefore develop.
  • SSFP magnetic resonance sequences are typically very sensitive to different phase positions of spins at the beginning of a repetition time.
  • the inventive approach which ensures correct refocusing of the spins, is particularly advantageous so that artifact-free and strong-signal magnetic resonance data can be acquired and reconstructed by an SSFP magnetic resonance sequence in vicinity of an interference object.
  • the magnetic resonance raw data are recorded by a quantitative magnetic resonance method.
  • a quantitative magnetic resonance method which is used to acquire the magnetic resonance image data, is used in particular for determining at least one quantitative material parameter.
  • the at least one material parameter is quantified in particular in a spatially resolved manner. A spatially resolved distribution of the at least one material parameter is therefore quantified.
  • the at least one material parameter advantageously characterizes a physical property of the material, for example of the tissue, from which the magnetic resonance signals originate.
  • the at least one material parameter can quantify a reaction of the material to the radio-frequency excitation.
  • a choice of potential material parameters, which can be quantified in the quantitative magnetic resonance method is: T 1 relaxation time, T 2 relaxation time, a diffusion value (for example an apparent diffusion coefficient, ADC), a magnetization moment, the proton density, the resonance frequency, a concentration of a material, etc. Further material parameters that are considered expedient to those skilled in the art are also conceivable. Any combination of the material parameters can be determined in the quantitative magnetic resonance method.
  • a quantitative magnetic resonance method advantageously enables quantification of the at least one material parameter, which is, for example, independent of scan conditions or type of magnetic resonance device. The quantification of the at least one material parameter therefore can be independent of parameter settings, adjustment scans, coil intensities, software versions, etc.
  • a quantitative magnetic resonance image, reconstructed from the magnetic resonance raw data acquired in the quantitative magnetic resonance method can therefore contain information about absolute physical variables.
  • the value of an image pixel of a quantitative magnetic resonance image of this kind therefore advantageously has a direct correlation with a physical measured value.
  • the value of an image pixel can have a physical unit. Therefore magnetic resonance images, respectively reconstructed from raw data acquired with different quantitative magnetic resonance methods, and potentially under different scan conditions, can advantageously be directly compared with each other. It is precisely in a quantitative magnetic resonance method that it is important to use a defined magnetic resonance sequence, since absolute physical variables are to be determined. A disrupted phase position of spins in a quantitative magnetic resonance method can lead to a falsification of the quantitative values of the at least one material parameter.
  • the inventive method can ensure this if it is used in combination with recording of quantitative magnetic resonance image data. Comparability of the quantitative magnetic resonance image data therefore can be ensured. It can also be ensured that the material parameters are correctly quantified in the quantitative magnetic resonance image data. In this way, exact quantitative magnetic resonance imaging is also possible in the vicinity of the interference object.
  • the quantitative magnetic resonance method is a magnetic resonance fingerprinting method, wherein, during each repetition interval of the multiple repetition intervals, data for a magnetic resonance image are acquired and a magnetic resonance signal characteristic is generated from the magnetic resonance images generated in this way. A signal comparison of the generated magnetic resonance signal characteristic takes place with a number of database signal characteristics stored in a database.
  • One possible magnetic resonance fingerprinting method is known, for example, from Ma et al., “Magnetic Resonance Fingerprinting”, Nature, 495, 187-192 (14 Mar. 2013).
  • various recording parameters are typically set for acquiring raw data for the magnetic resonance images. For each magnetic resonance image among the multiple magnetic resonance images detecting a number of spatially resolved magnetic resonance signal values are detected.
  • the magnetic resonance images are typically not intended to be made available, for example on a display monitor.
  • the recording parameters can be varied during detection of the multiple magnetic resonance images in a pseudo-randomized manner. Possible recording parameters, which are changed during the acquisition of the multiple magnetic resonance images, are echo time, the configuration and/or number of radio-frequency pulses, the configuration and/or number of gradient pulses, a diffusion encoding, etc.
  • a spatially-dependent magnetic resonance signal characteristic is then typically generated by the multiple magnetic resonance images. The magnetic resonance signal characteristic therefore indicates a change in recorded magnetic resonance signal values over the duration of detection of the magnetic resonance signal characteristic.
  • a time resolution of the magnetic resonance signal characteristic is formed by an interval between detection of two magnetic resonance images of the multiple magnetic resonance images, i.e. by the duration of a repetition interval.
  • This magnetic resonance signal characteristic is then typically compared in a signal comparison with a number of database signal characteristics stored in a database.
  • a different database value respectively of at least one material parameter is respectively allocated to the different database signal characteristics.
  • the database signal characteristic then constitutes the signal characteristic that is to be expected in the magnetic resonance fingerprinting method a sample is being examined, whose material properties match those of the associated database value of the at least one material parameter.
  • the database signal characteristics can be ascertained, for example, in a calibration scan and/or can be simulated.
  • a database signal characteristic of the multiple database signal characteristics is allocated to the generated magnetic resonance signal characteristic, using the result of the signal comparison.
  • the database value pertaining to the associated database signal characteristic of the at least one material parameter can then be set as the scan value of the at least one material parameter.
  • the reason for this is that interference to the refocusing of the spins by an interference object is typically not taken into account in the database signal characteristics.
  • the presence of the interference object can therefore lead to errors in the quantification of the material parameters by the magnetic resonance fingerprinting method.
  • the proposed compensation gradient can therefore ensure that the spins for the magnetic resonance fingerprinting method are correctly refocused at the end of each repetition interval. In this way the magnetic resonance signal characteristics can be correctly allocated to database signal characteristics and therefore the at least one material parameter can be correctly quantified by the magnetic resonance fingerprinting method in the vicinity of the interference object.
  • adjustment data are detected, and parameters of the magnetic compensation gradient are ascertained using the adjustment data.
  • the adjustment data can be used to identify inhomogeneities in the basic magnetic field, particularly after the examination object is positioned in the magnetic resonance scanner. Methods for detecting the adjustment data are known to those skilled in the art so such methods need not be discussed in detail herein.
  • a gradient moment of the magnetic compensation gradient can be ascertained using the adjustment data.
  • the gradient moment of the compensation gradient can be adjusted so as to be higher, the greater the inhomogeneity of the basic magnetic field is.
  • the adjustment data can therefore indirectly provide a conclusion about the magnetic interference field to be expected in the magnetic resonance imaging, which is caused by the interference object.
  • the adjustment data therefore represent a particularly advantageous starting point, using which the parameters of the magnetic compensation gradient can be set.
  • a B0 field map of the examination region can be detected, with parameters of the magnetic compensation gradient being ascertained using the B0 field map.
  • a B0 field map represents the field distribution of a main magnetic field of the magnetic resonance device.
  • the B0 field map is proportional to the basic magnetic field (B0 field) of the magnetic resonance device.
  • Other adjustment data for example frequency adjustment data, are also conceivable for ascertaining the parameters of the compensation gradient.
  • the acquisition of the magnetic resonance raw data includes emitting radio-frequency excitation pulses with an excitation frequency, with the excitation frequency being chosen such that it matches the resonance frequency of spins in a physical environment of the interference object.
  • the excitation frequency is chosen such that it matches the resonance frequency of spins in a physical environment of the interference object.
  • Matching the excitation frequency to the resonance frequency of the spins in the physical environment of the interference object can ensure that only the spins in the physical environment of the interference object are excited. Therefore, the magnetic resonance image data are reconstructed solely from magnetic resonance signals that originate from spins in the physical environment of the interference object. In this way the examination region can be efficiently matched to the physical environment of the interference object.
  • the magnetic resonance raw data can be acquired with the excitation frequency, which is matched to the resonance frequency of the spins in the physical environment of the interference object, as a final scan following acquisition of further magnetic resonance image data from a larger examination region, which includes the interference object. In this way, the vicinity of the interference object can again be purposefully imaged free from interference.
  • the invention also includes a magnetic resonance apparatus that has a scanner operated by a control computer that has an arithmetic module and a compensation gradient module configured to carry out the inventive method.
  • the magnetic resonance apparatus is therefore designed to carry out a method for magnetic resonance imaging an examination region of an examination object, wherein an interference object is situated in the examination region, which causes a magnetic interference field during raw magnetic resonance data acquisition.
  • the scanner of the magnetic resonance apparatus is operates to acquire magnetic resonance raw data from the examination region by execution of a magnetic resonance sequence that includes multiple repetition intervals and refocusing of spins in the examination region at the end of each repetition interval.
  • the compensation gradient module is configured to switch a magnetic compensation gradient that is opposed to the magnetic interference field, during at least part of the duration of the acquisition of the magnetic resonance raw data.
  • the compensation gradient module is designed to activate the magnetic compensation gradient so that interference, caused by the magnetic interference field, to the refocusing of the spins in the examination region is at least partially compensated.
  • the compensation gradient module is designed to activate the compensation gradient for the entire duration of acquisition of the magnetic resonance raw data.
  • the compensation gradient module is designed to activate the compensation gradient during refocusing of the spins in the examination region at the end of each repetition interval of the multiple repetition intervals.
  • the magnetic resonance apparatus has a refocusing gradient module that activates a refocusing gradient that refocuses the spins in the examination region by producing a gradient-induced phase development of the spins in the examination region, and the compensation gradient is activated during the refocusing gradient in addition to the refocusing gradient.
  • the compensation gradient module and the refocusing gradient module are designed such that parameters of the compensation gradient are ascertained as a function of parameters of the refocusing gradient.
  • the scanner is operated to execute, as the aforementioned magnetic resonance sequence, a steady-state free precession (SSFP) magnetic resonance sequence.
  • SSFP steady-state free precession
  • the scanner is operated to acquire the magnetic resonance raw data by a quantitative magnetic resonance method.
  • the scanner is operated with the quantitative magnetic resonance method being a magnetic resonance fingerprinting method, wherein raw data for a magnetic resonance image are acquired during each repetition interval of the multiple repetition intervals, and a magnetic resonance signal characteristic is generated from the magnetic resonance images of the respective intervals, and a signal comparison of the generated magnetic resonance signal characteristic is made with a number of database signal characteristics stored in a database.
  • the quantitative magnetic resonance method being a magnetic resonance fingerprinting method, wherein raw data for a magnetic resonance image are acquired during each repetition interval of the multiple repetition intervals, and a magnetic resonance signal characteristic is generated from the magnetic resonance images of the respective intervals, and a signal comparison of the generated magnetic resonance signal characteristic is made with a number of database signal characteristics stored in a database.
  • the magnetic resonance apparatus has an adjustment data acquisition module, wherein the adjustment data acquisition module and the compensation gradient module are designed to cause adjustment data to be acquired before acquiring the magnetic resonance raw data, and parameters of the magnetic compensation gradient are ascertained using the adjustment data.
  • the scanner is operated so that acquisition of the magnetic resonance raw data includes emitting radio-frequency excitation pulses with an excitation frequency, and the excitation frequency is chosen so as to match the resonance frequency of spins in a physical environment of the interference object.
  • the invention also encompasses a non-transitory, computer-readable data storage medium that can be loaded directly into a memory of a programmable arithmetic module of the control computer of the magnetic resonance apparatus.
  • the storage medium is encoded with programming instructions that cause the inventive method to be executed by the arithmetic module.
  • the inventive method can consequently be carried out quickly, robustly and in a manner that can be identically repeated.
  • the arithmetic module has an appropriate main memory, an appropriate graphics card or an appropriate logic unit, so the respective method steps can be carried out efficiently.
  • Examples of the electronically readable data storage medium are a DVD, a magnetic tape or a USB stick, on which electronically readable control information, in particular software, is stored.
  • FIG. 1 schematically illustrates an inventive magnetic resonance apparatus.
  • FIG. 2 is a flowchart of a first embodiment of the inventive method.
  • FIG. 3 is a flowchart of a second embodiment of the inventive method.
  • FIG. 4 illustrates a magnetic resonance sequence used in a third embodiment of the inventive method.
  • FIG. 5 illustrates a magnetic resonance sequence used in a fourth embodiment of the inventive method.
  • FIG. 1 schematically illustrates an inventive magnetic resonance apparatus 11 .
  • the magnetic resonance apparatus 11 has a scanner formed by a magnet unit 13 that has a basic field magnet 17 for generating a strong and constant basic magnetic field 18 .
  • the scanner has a cylindrical patient-receiving region 14 for receiving an examination object 15 , in the present case a patient, with the patient-receiving region 14 being cylindrically surrounded in a circumferential direction by the magnet unit 13 .
  • the patient 15 can be moved by a patient-positioning device 16 of the magnetic resonance apparatus 11 into the patient-receiving region 14 .
  • the patient-positioning device 16 has for this purpose an examination table arranged so as to move inside the scanner.
  • the magnet unit 13 is shielded from the outside by a housing shell 31 .
  • the magnet unit 13 also has a gradient coil unit 1 for generating magnetic field gradients which are used for spatial encoding during imaging.
  • the gradient coil module 19 is controlled by a gradient control module 28 .
  • the magnet unit 13 also has a radio-frequency antenna unit 20 , which in the illustrated case is designed as a body coil permanently integrated in the magnet unit 13 , and a radio-frequency antenna control module 29 for exciting nuclear spins in the patient 15 so as to depart from the polarization that is established in the basic magnetic field 18 generated by the basic field magnet 17 .
  • the radio-frequency antenna unit 20 is controlled by a radio-frequency antenna control module 29 so as to radiate radio-frequency magnetic resonance sequences into an examination space that is formed substantially by the patient-receiving region 14 .
  • the radio-frequency antenna unit 20 is also designed to receive magnetic resonance signals from the patient 15 .
  • the magnetic resonance apparatus 11 has an arithmetic processor 24 .
  • the arithmetic processor 24 centrally controls the magnetic resonance apparatus 11 , such as for example to execute a predetermined imaging gradient echo sequence. Control information such as imaging parameters, and reconstructed magnetic resonance images can be presented to a user at an interface, in the present case a display monitor 25 , of the magnetic resonance apparatus 11 .
  • the magnetic resonance apparatus 11 has an input unit 26 , via which information and/or parameters can be entered by a user during a scanning process.
  • the arithmetic processor 24 can include the gradient control module 28 and/or the radio-frequency antenna control module 29 and/or the display monitor 25 and/or the input unit 26 .
  • the gradient control module 28 has a compensation gradient module 33 .
  • the magnetic resonance apparatus 11 also has an image data recording module 32 .
  • the image data recording module 32 is formed by the magnet unit 13 together with the radio-frequency antenna control unit 29 and gradient control module 28 .
  • the magnetic resonance apparatus 11 is therefore configured, together with the image data recording module 32 , arithmetic processor 24 and compensation gradient module 33 , to implement an inventive method for magnetic resonance imaging.
  • the illustrated magnetic resonance apparatus 11 can have further components that magnetic resonance apparatuses conventionally have.
  • the general operation of a magnetic resonance apparatus is known to those skilled in the art, so a detailed description of the further components is not necessary herein.
  • FIG. 2 is a flowchart of a first embodiment of the inventive method for magnetic resonance imaging.
  • a magnetic resonance sequence is conventionally chosen and prepared. This means that, typically, a user determines the type of magnetic resonance sequence by way of an input unit 26 and/or chooses an appropriate protocol in which a specific magnetic resonance sequence is defined.
  • the examination object 15 is positioned in the magnetic resonance apparatus 11 and an examination region of the examination object 15 determined.
  • An interference object is positioned in the examination region. This interference object causes a magnetic interference field in magnetic resonance imaging.
  • magnetic resonance image data is recorded by means of the image data recording module 32 of the magnetic resonance apparatus 11 from the examination region by means of the magnetic resonance sequence.
  • the magnetic resonance sequence has multiple of repetition intervals and refocusing R of spins in the examination region at the end of each repetition interval of the plurality of repetition intervals in each case.
  • a magnetic compensation gradient C is also switched which is opposed to the magnetic interference field.
  • the compensation gradient C is switched by the gradient coil module 19 , wherein, for switching the compensation gradient C, the gradient coil module 19 is controlled by the compensation gradient module 33 of the gradient control module 19 .
  • the compensation gradient C is in particular switched so as to be overlaid with spatial encoding gradients provided by the magnetic resonance sequence, with the spatial encoding gradients also being switched by the gradient coil module 19 .
  • step 42 the recorded magnetic resonance image data are displayed for a user on the display monitor 25 and/or stored in a database.
  • FIG. 3 is a flowchart of a second embodiment of the inventive method for magnetic resonance imaging.
  • the embodiment of the inventive method shown in FIG. 3 substantially includes the method steps 40 , 41 , 42 of the first embodiment of the inventive method according to FIG. 2 .
  • the embodiment of the inventive method shown in FIG. 3 has additional method steps and/or substeps.
  • An alternative procedure to that in FIG. 3 which has only some of the additional method steps and/or substeps shown in FIG. 2 , is also conceivable.
  • an alternative procedure to that in FIG. 3 can also have additional method steps and/or substeps.
  • the magnetic resonance sequence chosen in further method step 40 can be a steady-state free precession (SSFP) magnetic resonance sequence.
  • SSFP steady-state free precession
  • the magnetic resonance sequence chosen in further method step 40 has refocusing of a gradient-induced phase development of the spins in the examination region by means of refocusing gradient R.
  • the refocusing gradient R is switched in particular by a refocusing gradient unit of the gradient control module 28 .
  • parameters of the refocusing gradient R are read out by means of the arithmetic processor 24 . These parameters of the refocusing gradient R are passed to the compensation gradient module 33 .
  • the compensation gradient module 33 ascertains parameters of the compensation gradient C in further method step 43 as a function of parameters of the refocusing gradient R.
  • the ascertained parameters of the magnetic compensation gradient C can then be set for the compensation gradient C during recording of the magnetic resonance image data in further method step 41 .
  • adjustment data is in a further method step 44 a by an adjustment data acquisition unit of the magnetic resonance device.
  • a B0 field map is acquired.
  • the field map is acquired in a further method step 44 a before recording of the magnetic resonance image data in further method step 41 .
  • the adjustment data is passed from the adjustment data acquisition unit to a parameter adjustment unit.
  • the parameter adjustment unit can ascertain parameters of the magnetic compensation gradient C in a further method step 44 b using the detected B0 field map by the arithmetic processor 24 .
  • the ascertained parameters of the magnetic compensation gradient C can then be set for the compensation gradient C during recording of the magnetic resonance image data in a further method step 41 .
  • the parameters of the parameter adjustment unit are transmitted to the gradient control module 28 of the magnetic resonance apparatus 11 .
  • the gradient control module 28 can then control the gradient coil module 19 using the parameters of the magnetic compensation gradient.
  • the compensation gradient C is switched by means of the compensation gradient module 33 during the refocusing gradient R.
  • the compensation gradient C can be switched throughout the entire duration of recording of the magnetic resonance image data.
  • the compensation gradient C can be purposefully switched for refocusing of the spins in the examination region at the end of each repetition interval of the plurality of repetition intervals.
  • the magnetic compensation gradient C is switched in a further method step 41 such that interference, caused by the magnetic interference field, to the refocusing of the spins is at least partially compensated in the examination region.
  • Recording of the magnetic resonance image data in further method step 41 by means of the image data recording module 32 also comprises emitting radio-frequency excitation pulses E with an excitation frequency, with the excitation frequency being chosen such that it matches a resonance frequency of spins in a physical environment of the interference object.
  • the radio-frequency excitation pulses E which are emitted in particular by means of an excitation pulse unit of the magnetic resonance apparatus 11 .
  • the magnetic resonance image data is recorded in a further method step 41 , for example by a quantitative magnetic resonance method.
  • the quantitative magnetic resonance method is a magnetic resonance fingerprinting method.
  • a magnetic resonance image is recorded by means of the image data recording module 32 during each repetition interval of the plurality of repetition intervals.
  • the magnetic resonance fingerprinting method includes in particular that recording parameters that have been changed in a pseudo randomized manner are used during recording of the magnetic resonance images.
  • the number of magnetic resonance images recorded in this way are not displayed directly but processed further in a further method step 45 by the arithmetic processor 24 .
  • a magnetic resonance signal characteristic is generated from the recorded magnetic resonance images.
  • one signal characteristic is formed by each voxel of the magnetic resonance images over the plurality of magnetic resonance images.
  • a second substep 45 b of the further method step 45 there is a signal comparison of the generated magnetic resonance signal characteristic with a number of database signal characteristics stored in a database.
  • a database value of at least one tissue parameter is allocated to each database signal characteristic of the number of database signal characteristics.
  • the database is connected in particular in the sense of a data exchange to the arithmetic processor 24 .
  • the magnetic resonance signal characteristic is compared by way of example with each of the database signal characteristics.
  • the signal comparison can occur by a conventional pattern recognition method and/or by a correlation analysis.
  • a comparison parameter is then output for each comparison, and this characterizes the degree of accord between the magnetic resonance signal characteristic and the database signal characteristics.
  • tissue parameter map can be created in this way in a third substep 45 c, and this includes a spatially resolved distribution of the at least one tissue parameter in the examination region.
  • the content of the tissue parameter map is determined by way of example such that an appropriate database signal characteristic of the number of database signal characteristics is ascertained for the magnetic resonance signal characteristic.
  • the appropriate database signal characteristic has in particular the greatest accord with the magnetic resonance signal characteristic.
  • a database value of the at least one tissue parameter linked to the appropriate database signal characteristic can then be included in the tissue parameter map.
  • This method can be repeated for each magnetic resonance signal characteristic of the various voxels of the magnetic resonance images, resulting in a spatially resolved distribution of the at least one tissue parameter.
  • the tissue parameter map can then be output in a further method step 42 on the display unit 25 and/or be stored in the database.
  • the method steps of the inventive method illustrated in FIGS. 2 to 3 are executed by the arithmetic processor 24 .
  • the arithmetic processor 24 comprises the required software and/or computer programs which are stored in a memory unit of the arithmetic processor 24 .
  • the software and/or computer programs comprise program means which are configured to carry out the inventive method when the computer program and/or the software is run in the arithmetic processor 24 by means of a processor unit of the arithmetic processor 24 .
  • FIG. 4 shows a magnetic resonance sequence used in a third embodiment of the inventive method.
  • FIG. 5 shows a magnetic resonance sequence used in a fourth embodiment of the inventive method.
  • sequences shown in FIG. 4 and FIG. 5 should only be regarded as examples and represent one possibility of how a sequence over time of the magnetic resonance sequence could look. Reference should also be made to the fact that the sequence plans shown in FIG. 4 and FIG. 5 are incomplete since, for example, the spatial encoding gradients and readout windows are not shown.
  • the sequence plans shown in FIG. 4 and FIG. 5 are also illustrated in an abstract manner. This means, only the chronology of sequence elements over time is shown and the exact formation of the sequence elements is not dealt with in detail.
  • time windows are in each case plotted on different time lines one above the other, in which windows the repetition intervals T, radio-frequency excitation pulses E, refocusing gradient R and compensation gradient C occur.
  • scaling in the time direction occurs only in arbitrary units for the purpose of simplification.
  • Both sequences as examples have three repetition intervals T 1 , T 2 , T 3 of the magnetic resonance sequence.
  • these repetition intervals T 1 , T 2 , T 3 represent only a section of the magnetic resonance sequence.
  • the magnetic resonance sequence will typically have more repetition intervals T for recording the magnetic resonance image data.
  • Each repetition interval T 1 , T 2 , T 3 begins with a radio-frequency excitation pulse E 1 , E 2 , E 3 .
  • E 1 , E 2 , E 3 At the end of each repetition interval T 1 , T 2 , T 3 there is a refocusing of spins in the examination region by means of refocusing gradient R 1 , R 2 , R 3 .
  • Interference caused by a magnetic interference field, to the refocusing of the spins in the examination region is at least partially compensated by compensation gradients C 1 , C 2 , C 3 , C′.
  • the compensation gradients C 1 , C 2 , C 3 , C′ are switched during at least part of the duration of recording of the magnetic resonance image data.
  • the compensation gradients C 1 , C 2 , C 3 , C′ are opposed to the magnetic interference field.
  • the compensation gradients C 1 , C 2 , C 3 are switched for refocusing the spins in the examination region at the end of each repetition interval T 1 , T 2 , T 3 .
  • the compensation gradients C 1 , C 2 , C 3 shown in the exemplary embodiment in FIG. 4 are only switched during the refocusing gradients R 1 , R 2 , R 3 .
  • a first compensation gradient C 1 of a first repetition interval Ti therefore occurs during a first refocusing gradient R 1 of the first repetition interval T 1 .
  • a second compensation gradient C 2 of a second repetition interval T 2 therefore occurs during a second refocusing gradient R 2 of the second repetition interval T 2 .
  • a third compensation gradient C 3 of a third repetition interval T 3 therefore occurs during a third refocusing gradient R 3 of the third repetition interval T 3 .
  • a compensation gradient C′ is switched for the entire duration of recording of the magnetic resonance image data.
  • the compensation gradient C′ according to FIG. 5 is switched not just during the refocusing gradients R 1 , R 2 , R 3 , but also for the remaining duration of the multiple repetition intervals T 1 , T 2 , T 3 .

Abstract

To enable improved magnetic resonance imaging in the vicinity of an interference object that produces a magnetic interference field in an examination region, in a method and apparatus for magnetic resonance imaging of the examination region magnetic resonance raw data are acquired from the examination region by execution of a magnetic resonance sequence having multiple repetition intervals and refocusing of spins in the examination region at the end of each repetition interval repetition intervals. During at least part of the duration of the acquisition of the magnetic resonance raw data, a magnetic compensation gradient is activated that is opposed to the magnetic interference field.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The invention concerns a method for magnetic resonance imaging, a magnetic resonance apparatus and a computer-readable data storage medium.
  • 2. Description of the Prior Art
  • In a magnetic resonance apparatus, also called a magnetic resonance tomography system, the body to be examined of an examination subject, in particular a patient, is conventionally exposed with the use of a basic field magnet to a relatively high basic magnetic field, for example of 1.5 or 3 or 7 tesla. In addition, gradient switching operations occur with a gradient coil unit. Radio-frequency pulses, in particular excitation pulses, are then emitted by a radio-frequency antenna unit via suitable antennas, and this leads to the nuclear spins (spins) of specific atoms excited in a resonant manner by these radio-frequency pulses being tilted by a defined flip angle with respect to the magnetic field lines of the basic magnetic field. When the spins are relaxed, radio-frequency signals, known as magnetic resonance signals, are emitted from the spins, and these are received by a suitable radio-frequency antenna, and then processed further. The desired image data can be reconstructed from the raw data acquired in this way.
  • For a specific scan a specific magnetic resonance sequence, also called a pulse sequence, should be emitted, which includes a series of radio-frequency pulses, in particular radio-frequency excitation pulses, and gradient switching operations, which are activated in appropriate coordination with the radio-frequency pulses along different gradient axes in different spatial directions. Readout windows that are appropriately timed are set, which specify the periods in which the induced magnetic resonance signals are detected.
  • An interference object may be present in an examination region of a magnetic resonance recording. This interference object is characterized by having a magnetic susceptibility that differs from the magnetic susceptibility of tissue surrounding the interference object. This interference object therefore can lead to magnetic interference fields that can make imaging of the interference object difficult and/or lead to image artifacts in the vicinity of the interference object.
  • SUMMARY OF THE INVENTION
  • An object of the invention is to enable improved magnetic resonance imaging in the vicinity of an interference object.
  • According to the invention, in a method for acquiring magnetic resonance raw data from an examination region of an examination object by operation of a magnetic resonance scanner, wherein an interference object is situated in the examination region that causes a magnetic interference field during magnetic resonance data acquisition, magnetic resonance raw data are acquired from the examination region by execution of a magnetic resonance sequence having multiple repetition intervals with refocusing of nuclear spins in the examination region at the end of each repetition interval, and wherein, during at least part of the duration of acquisition of the magnetic resonance raw data, a magnetic compensation gradient is activated that is opposed to the magnetic interference field.
  • The examination object can be a patient, a trainee or a phantom. The examination region, also called the field of view (FOV) is a volume of which an image is to be reconstructed from the acquired raw magnetic resonance data. The reconstructed magnetic resonance image is presented, i.e. displayed on a display monitor for a user and/or stored in a database. In either case, the raw data are compiled in a datafile in a memory during acquisition thereof, and the image data are also compiled in a datafile.
  • The interference object has a magnetic susceptibility that differs from the magnetic susceptibility of the material that surrounds the interference object. The interference object in particular has a magnetic susceptibility that is different from the magnetic susceptibility of surrounding tissue of the examination object in the examination region. In particular, the magnetic susceptibility of the interference object is higher than, often more than ten times higher than, the magnetic susceptibility of the material that surrounds the interference object. The interference object can include metal. The interference object can be, for example, a metallic implant in the examination object, such as an artificial hip joint.
  • The magnetic interference field of the interference object is produced due to the difference of the susceptibility of the interference object from the surrounding material. The magnetic interference field can have a magnetic field gradient. The magnetic interference field therefore can lead to at least one additional gradient moment being present during acquisition of the raw data. The magnetic interference field of the interference object therefore can disrupt the nuclear spins that are excited during the magnetic resonance raw data acquisition. The magnetic interference field typically disrupts a phase development and/or a phase position of the spins. This can mean that the excited spins are dephased due to the magnetic interference field, in particular drift apart. In this way the interference object can lead to a signal loss in the recorded magnetic resonance raw data in a vicinity of the interference object. In this way the magnetic interference field can disrupt refocusing of the spins.
  • The multiple repetition intervals in the magnetic resonance sequence will each have a duration of one repetition time. The repetition time is typically defined as the duration that occurs between two radio-frequency excitation pulses of the magnetic resonance sequence. The magnetic resonance sequence is advantageously designed as a single-shot magnetic resonance sequence. This means that the magnetic resonance raw data produce a number of magnetic resonance images. In each repetition interval among the multiple repetition intervals, raw data are acquired for reconstruction of one magnetic resonance image among the multiple magnetic resonance images. The respective sets of raw data for the multiple magnetic resonance images are acquired consecutively, within a portion of each repetition time.
  • In the case of a spin echo magnetic resonance sequence, the spins can be refocused by a radio-frequency refocusing pulse. In the case of a gradient echo magnetic resonance sequence, the spins can be refocused by a refocusing gradient switching operation, also called refocusing gradient. The refocusing gradient is switched in the phase encoding direction. Refocusing of the spins leads to a defined starting position (angle) of the spins at the beginning of a repetition interval. Refocusing of the spins conventionally involves refocusing dephased spins. Refocusing of the spins may also include a different change in the phase position of the spins.
  • The magnetic interference field of the interference object can disrupt this refocusing of the spins. To compensate the magnetic interference field at least partially, the compensation gradient in accordance with the invention is activated. The magnetic compensation gradient is switched by the gradient coils that are conventionally present in the magnetic resonance scanner. The compensation gradient is designed as a magnetic gradient field. The compensation gradient is switched with the spatial encoding gradients in an overlaid manner, these spatial encoding gradients already being present in the magnetic resonance sequence. The compensation gradient may also be switched in an overlaid manner on a refocusing gradient. The compensation gradient is therefore switched (activated) in addition to the spatial encoding gradient and/or the refocusing gradient. The fact that the magnetic compensation gradient is opposed to the magnetic interference field means that there is an increase in the magnetic compensation gradient in a direction that is opposite to the direction of increase in the magnetic interference field. The gradient moment of the compensation gradient is also designed so as to be opposed to the gradient moment of the magnetic interference field. The gradient moment is typically defined by the time integral of the amplitude of a gradient switching operation.
  • Interference to the refocusing of the spins due to the magnetic interference field can be at least partially prevented by the approach according to the invention. The compensation gradient can ensure that the spins are more correctly refocused at the end of each repetition interval of the multiple repetition intervals. Thus there can be a macro-defined starting point for a phase position of the spins at the beginning of the multiple repetition intervals. The raw data for each magnetic resonance image among the multiple magnetic resonance images thus are acquired, in each repetition interval of the multiple repetition intervals, on a comparable basis and/or under standardized boundary conditions. In this way magnetic resonance imaging can be carried out particularly effectively in the vicinity of the interference object. It is also possible for artifact-reduced magnetic resonance image data to be generated with the method according to the invention. In particular in the immediate vicinity of the interference object, the tissue of the examination object can be correctly shown in the magnetic resonance image data.
  • A number of sets of magnetic resonance raw data from the examination region can be acquired in a number of magnetic resonance scans. A different compensation gradient can then be switched during each raw data set acquisition to compensate a different magnetic interference field. A first set of magnetic resonance raw data therefore can be acquired in a first magnetic resonance scan using a first compensation gradient that compensates a first magnetic interference field, and in a second magnetic resonance scan, a second set of magnetic resonance raw data can be acquired using a second compensation gradient that compensates a second magnetic interference field. Different interference fields, which are caused by one or more interference object(s) in the examination region, can thereby be particularly accurately compensated.
  • In an embodiment, the magnetic compensation gradient is switched such that interference, caused by the magnetic interference field, to the refocusing of the spins in the examination region is at least partially compensated. For this purpose, the gradient moment of the magnetic compensation gradient is chosen such that the gradient moment of the magnetic interference field is at least partially compensated. This can ensure extensive, possibly complete, refocusing of the spins in the examination region. The extensive, in particular complete, refocusing of the spins is then present at the beginning of each repetition interval of the multiple repetition intervals.
  • In another embodiment, the compensation gradient is switched for the entire duration of acquisition of the magnetic resonance raw data. In particular, the compensation gradient is then switched for the entire repetition interval. In this way a disruptive gradient moment of the magnetic interference field can be reliably compensated throughout the entire recording of the magnetic resonance image data.
  • In another embodiment, the compensation gradient is switched during refocusing of the spins in the examination region at the end of each repetition interval of the multiple repetition intervals. The compensation gradient is therefore advantageously switched only if refocusing of the spins occurs. The compensation gradient is therefore advantageously activated in precisely that period during which refocusing of the spins occurs. The compensation gradient is switched only at the end of each repetition interval. It is advantageous to switch the compensation gradient selectively during refocusing because a dephasing of spins, produced by the compensation gradient, which are not affected by the magnetic interference field, can therefore be at least partially prevented and/or reduced. The compensation gradient thus can advantageously be matched to the requirements for refocusing of the spins.
  • In another embodiment, refocusing of the spins in the examination region includes refocusing of a gradient-induced phase development of the spins in the examination region by a refocusing gradient, and the compensation gradient is switched during the refocusing gradient in addition to the refocusing gradient. The refocusing gradient is switched in the phase encoding direction, so the gradient-induced phase development of the spins can be refocused. The compensation gradient is then switched in addition to the refocusing gradient, so the interference in the phase development of the spins, caused by the interference object, can be at least partially compensated. This approach is based on the concept that the refocusing gradient is typically fixed by the magnetic resonance sequence. The refocusing gradient therefore typically cannot be variably adjusted to the presence of the interference object in the examination region. The compensation gradient can then advantageously take on this task. The compensation gradient can modulate the refocusing gradient so an optimum refocusing of the spins in the examination region can be attained, while taking account of the magnetic interference field of the interference object. The refocusing gradient and the compensation gradient are switched in an overlaid manner by the gradient coil, so an effective compensation-refocusing gradient switching operation is carried out at the end of each repetition interval of the multiple repetition intervals.
  • In another embodiment, parameters of the compensation gradient are ascertained as a function of parameters of the refocusing gradient. Parameters of a gradient switching operation can be, for example, the amplitude of the gradient switching operation, the duration of the gradient switching operation, the slew rate of the gradient switching operation, etc. Further parameters of the gradient switching operation that sre4 considered expedient by those skilled in the art are also conceivable. The compensation gradient can be advantageously matched to the refocusing gradient by ascertaining the parameters of the compensation gradient as a function of the parameters of the refocusing gradient. The spins in the examination region can be particularly effectively refocused in this way.
  • In another embodiment, the magnetic resonance sequence is a steady-state free precession (SSFP) magnetic resonance sequence. An SSFP magnetic resonance sequence typically includes a sequence of radio-frequency excitation pulses with the condition that the repetition time, i.e. the duration of a repetition interval, is less than the T2 relaxation time of the relevant tissue of the examination object. The radio-frequency excitation pulses are therefore switched in an interval, the repetition time, which is smaller than the T2 time. Magnetization of the spins in the steady state can therefore develop. SSFP magnetic resonance sequences are typically very sensitive to different phase positions of spins at the beginning of a repetition time. In the case of SSFP magnetic resonance sequences, it may therefore be expedient to carry out refocusing of the phase development of the spins at the end of the repetition intervals. The steady state can develop particularly reliably in this way. In this way the inventive approach, which ensures correct refocusing of the spins, is particularly advantageous so that artifact-free and strong-signal magnetic resonance data can be acquired and reconstructed by an SSFP magnetic resonance sequence in vicinity of an interference object.
  • In another embodiment, the magnetic resonance raw data are recorded by a quantitative magnetic resonance method. A quantitative magnetic resonance method, which is used to acquire the magnetic resonance image data, is used in particular for determining at least one quantitative material parameter. The at least one material parameter is quantified in particular in a spatially resolved manner. A spatially resolved distribution of the at least one material parameter is therefore quantified. The at least one material parameter advantageously characterizes a physical property of the material, for example of the tissue, from which the magnetic resonance signals originate. In particular, the at least one material parameter can quantify a reaction of the material to the radio-frequency excitation. A choice of potential material parameters, which can be quantified in the quantitative magnetic resonance method, is: T1 relaxation time, T2 relaxation time, a diffusion value (for example an apparent diffusion coefficient, ADC), a magnetization moment, the proton density, the resonance frequency, a concentration of a material, etc. Further material parameters that are considered expedient to those skilled in the art are also conceivable. Any combination of the material parameters can be determined in the quantitative magnetic resonance method. A quantitative magnetic resonance method advantageously enables quantification of the at least one material parameter, which is, for example, independent of scan conditions or type of magnetic resonance device. The quantification of the at least one material parameter therefore can be independent of parameter settings, adjustment scans, coil intensities, software versions, etc. A quantitative magnetic resonance image, reconstructed from the magnetic resonance raw data acquired in the quantitative magnetic resonance method, can therefore contain information about absolute physical variables. The value of an image pixel of a quantitative magnetic resonance image of this kind therefore advantageously has a direct correlation with a physical measured value. The value of an image pixel can have a physical unit. Therefore magnetic resonance images, respectively reconstructed from raw data acquired with different quantitative magnetic resonance methods, and potentially under different scan conditions, can advantageously be directly compared with each other. It is precisely in a quantitative magnetic resonance method that it is important to use a defined magnetic resonance sequence, since absolute physical variables are to be determined. A disrupted phase position of spins in a quantitative magnetic resonance method can lead to a falsification of the quantitative values of the at least one material parameter. Therefore, it is specifically in a quantitative magnetic resonance method, which uses refocusing of the spins, that it is important for the refocusing of the spins to occur correctly. The inventive method can ensure this if it is used in combination with recording of quantitative magnetic resonance image data. Comparability of the quantitative magnetic resonance image data therefore can be ensured. It can also be ensured that the material parameters are correctly quantified in the quantitative magnetic resonance image data. In this way, exact quantitative magnetic resonance imaging is also possible in the vicinity of the interference object.
  • In another embodiment, the quantitative magnetic resonance method is a magnetic resonance fingerprinting method, wherein, during each repetition interval of the multiple repetition intervals, data for a magnetic resonance image are acquired and a magnetic resonance signal characteristic is generated from the magnetic resonance images generated in this way. A signal comparison of the generated magnetic resonance signal characteristic takes place with a number of database signal characteristics stored in a database. One possible magnetic resonance fingerprinting method is known, for example, from Ma et al., “Magnetic Resonance Fingerprinting”, Nature, 495, 187-192 (14 Mar. 2013). In a magnetic resonance fingerprinting method various recording parameters are typically set for acquiring raw data for the magnetic resonance images. For each magnetic resonance image among the multiple magnetic resonance images detecting a number of spatially resolved magnetic resonance signal values are detected. These signal values are present in the image region of an examination region. The signal values are not present in k-space. The magnetic resonance images are typically not intended to be made available, for example on a display monitor. The recording parameters can be varied during detection of the multiple magnetic resonance images in a pseudo-randomized manner. Possible recording parameters, which are changed during the acquisition of the multiple magnetic resonance images, are echo time, the configuration and/or number of radio-frequency pulses, the configuration and/or number of gradient pulses, a diffusion encoding, etc. A spatially-dependent magnetic resonance signal characteristic is then typically generated by the multiple magnetic resonance images. The magnetic resonance signal characteristic therefore indicates a change in recorded magnetic resonance signal values over the duration of detection of the magnetic resonance signal characteristic. A time resolution of the magnetic resonance signal characteristic is formed by an interval between detection of two magnetic resonance images of the multiple magnetic resonance images, i.e. by the duration of a repetition interval. This magnetic resonance signal characteristic is then typically compared in a signal comparison with a number of database signal characteristics stored in a database. A different database value respectively of at least one material parameter is respectively allocated to the different database signal characteristics. The database signal characteristic then constitutes the signal characteristic that is to be expected in the magnetic resonance fingerprinting method a sample is being examined, whose material properties match those of the associated database value of the at least one material parameter. The database signal characteristics can be ascertained, for example, in a calibration scan and/or can be simulated. In such a magnetic resonance fingerprinting method, typically a database signal characteristic of the multiple database signal characteristics is allocated to the generated magnetic resonance signal characteristic, using the result of the signal comparison. The database value pertaining to the associated database signal characteristic of the at least one material parameter can then be set as the scan value of the at least one material parameter. For detecting the magnetic resonance images according to the magnetic resonance fingerprinting method, it is typically necessary that the spins are refocused in the examination region at the end of each repetition interval. If this refocusing is disrupted by the presence of the interference object, a magnetic resonance signal characteristic detected in the vicinity of the interference object can be disrupted. Errors can consequently occur in the allocation of the magnetic resonance signal characteristic detected in vicinity of the interference object to the database signal characteristics. The reason for this is that interference to the refocusing of the spins by an interference object is typically not taken into account in the database signal characteristics. The presence of the interference object can therefore lead to errors in the quantification of the material parameters by the magnetic resonance fingerprinting method. The proposed compensation gradient can therefore ensure that the spins for the magnetic resonance fingerprinting method are correctly refocused at the end of each repetition interval. In this way the magnetic resonance signal characteristics can be correctly allocated to database signal characteristics and therefore the at least one material parameter can be correctly quantified by the magnetic resonance fingerprinting method in the vicinity of the interference object.
  • In another embodiment before acquiring the magnetic resonance raw data, adjustment data are detected, and parameters of the magnetic compensation gradient are ascertained using the adjustment data. The adjustment data can be used to identify inhomogeneities in the basic magnetic field, particularly after the examination object is positioned in the magnetic resonance scanner. Methods for detecting the adjustment data are known to those skilled in the art so such methods need not be discussed in detail herein. In particular, a gradient moment of the magnetic compensation gradient can be ascertained using the adjustment data. The gradient moment of the compensation gradient can be adjusted so as to be higher, the greater the inhomogeneity of the basic magnetic field is. The adjustment data can therefore indirectly provide a conclusion about the magnetic interference field to be expected in the magnetic resonance imaging, which is caused by the interference object. The adjustment data therefore represent a particularly advantageous starting point, using which the parameters of the magnetic compensation gradient can be set. For example, before acquiring the magnetic resonance raw data, a B0 field map of the examination region can be detected, with parameters of the magnetic compensation gradient being ascertained using the B0 field map. A B0 field map represents the field distribution of a main magnetic field of the magnetic resonance device. The B0 field map is proportional to the basic magnetic field (B0 field) of the magnetic resonance device. Other adjustment data, for example frequency adjustment data, are also conceivable for ascertaining the parameters of the compensation gradient.
  • In another embodiment, the acquisition of the magnetic resonance raw data includes emitting radio-frequency excitation pulses with an excitation frequency, with the excitation frequency being chosen such that it matches the resonance frequency of spins in a physical environment of the interference object. This is possible since the resonance frequency of the spins is shifted in the physical environment of the interference object by the presence of the interference object. Matching the excitation frequency to the resonance frequency of the spins in the physical environment of the interference object can ensure that only the spins in the physical environment of the interference object are excited. Therefore, the magnetic resonance image data are reconstructed solely from magnetic resonance signals that originate from spins in the physical environment of the interference object. In this way the examination region can be efficiently matched to the physical environment of the interference object. At the same time, refocusing of the spins in the physical environment of the interference object can be purposefully optimized by the magnetic compensation gradient. Thus there is no undesirable dephasing of spins that are situated at a distance from the interference object positioned, due to the compensation gradient. The magnetic resonance raw data can be acquired with the excitation frequency, which is matched to the resonance frequency of the spins in the physical environment of the interference object, as a final scan following acquisition of further magnetic resonance image data from a larger examination region, which includes the interference object. In this way, the vicinity of the interference object can again be purposefully imaged free from interference.
  • The invention also includes a magnetic resonance apparatus that has a scanner operated by a control computer that has an arithmetic module and a compensation gradient module configured to carry out the inventive method.
  • The magnetic resonance apparatus is therefore designed to carry out a method for magnetic resonance imaging an examination region of an examination object, wherein an interference object is situated in the examination region, which causes a magnetic interference field during raw magnetic resonance data acquisition. The scanner of the magnetic resonance apparatus is operates to acquire magnetic resonance raw data from the examination region by execution of a magnetic resonance sequence that includes multiple repetition intervals and refocusing of spins in the examination region at the end of each repetition interval. The compensation gradient module is configured to switch a magnetic compensation gradient that is opposed to the magnetic interference field, during at least part of the duration of the acquisition of the magnetic resonance raw data.
  • In an embodiment of the magnetic resonance apparatus, the compensation gradient module is designed to activate the magnetic compensation gradient so that interference, caused by the magnetic interference field, to the refocusing of the spins in the examination region is at least partially compensated.
  • In another embodiment of the magnetic resonance apparatus, the compensation gradient module is designed to activate the compensation gradient for the entire duration of acquisition of the magnetic resonance raw data.
  • In another embodiment of the magnetic resonance apparatus, the compensation gradient module is designed to activate the compensation gradient during refocusing of the spins in the examination region at the end of each repetition interval of the multiple repetition intervals.
  • In another embodiment of the magnetic resonance apparatus, the magnetic resonance apparatus has a refocusing gradient module that activates a refocusing gradient that refocuses the spins in the examination region by producing a gradient-induced phase development of the spins in the examination region, and the compensation gradient is activated during the refocusing gradient in addition to the refocusing gradient.
  • In another embodiment of the magnetic resonance apparatus, the compensation gradient module and the refocusing gradient module are designed such that parameters of the compensation gradient are ascertained as a function of parameters of the refocusing gradient.
  • In another embodiment of the magnetic resonance apparatus, the scanner is operated to execute, as the aforementioned magnetic resonance sequence, a steady-state free precession (SSFP) magnetic resonance sequence.
  • In a further embodiment of the magnetic resonance apparatus, the scanner is operated to acquire the magnetic resonance raw data by a quantitative magnetic resonance method.
  • In a version of this embodiment of the magnetic resonance apparatus the scanner is operated with the quantitative magnetic resonance method being a magnetic resonance fingerprinting method, wherein raw data for a magnetic resonance image are acquired during each repetition interval of the multiple repetition intervals, and a magnetic resonance signal characteristic is generated from the magnetic resonance images of the respective intervals, and a signal comparison of the generated magnetic resonance signal characteristic is made with a number of database signal characteristics stored in a database.
  • In another embodiment of the magnetic resonance apparatus, the magnetic resonance apparatus has an adjustment data acquisition module, wherein the adjustment data acquisition module and the compensation gradient module are designed to cause adjustment data to be acquired before acquiring the magnetic resonance raw data, and parameters of the magnetic compensation gradient are ascertained using the adjustment data.
  • In another embodiment of the magnetic resonance apparatus, the scanner is operated so that acquisition of the magnetic resonance raw data includes emitting radio-frequency excitation pulses with an excitation frequency, and the excitation frequency is chosen so as to match the resonance frequency of spins in a physical environment of the interference object.
  • The invention also encompasses a non-transitory, computer-readable data storage medium that can be loaded directly into a memory of a programmable arithmetic module of the control computer of the magnetic resonance apparatus. The storage medium is encoded with programming instructions that cause the inventive method to be executed by the arithmetic module. The inventive method can consequently be carried out quickly, robustly and in a manner that can be identically repeated. The arithmetic module has an appropriate main memory, an appropriate graphics card or an appropriate logic unit, so the respective method steps can be carried out efficiently. Examples of the electronically readable data storage medium are a DVD, a magnetic tape or a USB stick, on which electronically readable control information, in particular software, is stored.
  • The advantages of the inventive magnetic resonance apparatus and of the inventive storage medium correspond to the advantages of the inventive method, as discussed above in detail. Features, advantages or alternative embodiments mentioned in that context are applicable to the other aspects of the invention. The corresponding functional features of the method are implemented by appropriate modules, in particular by hardware modules.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 schematically illustrates an inventive magnetic resonance apparatus.
  • FIG. 2 is a flowchart of a first embodiment of the inventive method.
  • FIG. 3 is a flowchart of a second embodiment of the inventive method.
  • FIG. 4 illustrates a magnetic resonance sequence used in a third embodiment of the inventive method.
  • FIG. 5 illustrates a magnetic resonance sequence used in a fourth embodiment of the inventive method.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • FIG. 1 schematically illustrates an inventive magnetic resonance apparatus 11. The magnetic resonance apparatus 11 has a scanner formed by a magnet unit 13 that has a basic field magnet 17 for generating a strong and constant basic magnetic field 18. The scanner has a cylindrical patient-receiving region 14 for receiving an examination object 15, in the present case a patient, with the patient-receiving region 14 being cylindrically surrounded in a circumferential direction by the magnet unit 13. The patient 15 can be moved by a patient-positioning device 16 of the magnetic resonance apparatus 11 into the patient-receiving region 14. The patient-positioning device 16 has for this purpose an examination table arranged so as to move inside the scanner. The magnet unit 13 is shielded from the outside by a housing shell 31.
  • The magnet unit 13 also has a gradient coil unit 1 for generating magnetic field gradients which are used for spatial encoding during imaging. The gradient coil module 19 is controlled by a gradient control module 28. The magnet unit 13 also has a radio-frequency antenna unit 20, which in the illustrated case is designed as a body coil permanently integrated in the magnet unit 13, and a radio-frequency antenna control module 29 for exciting nuclear spins in the patient 15 so as to depart from the polarization that is established in the basic magnetic field 18 generated by the basic field magnet 17. The radio-frequency antenna unit 20 is controlled by a radio-frequency antenna control module 29 so as to radiate radio-frequency magnetic resonance sequences into an examination space that is formed substantially by the patient-receiving region 14. The radio-frequency antenna unit 20 is also designed to receive magnetic resonance signals from the patient 15.
  • For controlling the basic field magnet 17, the gradient control module 28 and the radio-frequency antenna control module 29, the magnetic resonance apparatus 11 has an arithmetic processor 24. The arithmetic processor 24 centrally controls the magnetic resonance apparatus 11, such as for example to execute a predetermined imaging gradient echo sequence. Control information such as imaging parameters, and reconstructed magnetic resonance images can be presented to a user at an interface, in the present case a display monitor 25, of the magnetic resonance apparatus 11. In addition, the magnetic resonance apparatus 11 has an input unit 26, via which information and/or parameters can be entered by a user during a scanning process. The arithmetic processor 24 can include the gradient control module 28 and/or the radio-frequency antenna control module 29 and/or the display monitor 25 and/or the input unit 26.
  • In the illustrated case the gradient control module 28 has a compensation gradient module 33. The magnetic resonance apparatus 11 also has an image data recording module 32. In the present case, the image data recording module 32 is formed by the magnet unit 13 together with the radio-frequency antenna control unit 29 and gradient control module 28. The magnetic resonance apparatus 11 is therefore configured, together with the image data recording module 32, arithmetic processor 24 and compensation gradient module 33, to implement an inventive method for magnetic resonance imaging.
  • The illustrated magnetic resonance apparatus 11 can have further components that magnetic resonance apparatuses conventionally have. The general operation of a magnetic resonance apparatus is known to those skilled in the art, so a detailed description of the further components is not necessary herein.
  • FIG. 2 is a flowchart of a first embodiment of the inventive method for magnetic resonance imaging.
  • In a first method step 40, a magnetic resonance sequence is conventionally chosen and prepared. This means that, typically, a user determines the type of magnetic resonance sequence by way of an input unit 26 and/or chooses an appropriate protocol in which a specific magnetic resonance sequence is defined. In a further method step 40 the examination object 15 is positioned in the magnetic resonance apparatus 11 and an examination region of the examination object 15 determined. An interference object is positioned in the examination region. This interference object causes a magnetic interference field in magnetic resonance imaging.
  • In a further method step 41 magnetic resonance image data is recorded by means of the image data recording module 32 of the magnetic resonance apparatus 11 from the examination region by means of the magnetic resonance sequence. The magnetic resonance sequence has multiple of repetition intervals and refocusing R of spins in the examination region at the end of each repetition interval of the plurality of repetition intervals in each case. During at least part of the duration recording of the magnetic resonance image data a magnetic compensation gradient C is also switched which is opposed to the magnetic interference field. The compensation gradient C is switched by the gradient coil module 19, wherein, for switching the compensation gradient C, the gradient coil module 19 is controlled by the compensation gradient module 33 of the gradient control module 19. The compensation gradient C is in particular switched so as to be overlaid with spatial encoding gradients provided by the magnetic resonance sequence, with the spatial encoding gradients also being switched by the gradient coil module 19.
  • In a further method step 42 the recorded magnetic resonance image data are displayed for a user on the display monitor 25 and/or stored in a database.
  • FIG. 3 is a flowchart of a second embodiment of the inventive method for magnetic resonance imaging.
  • The following description is substantially limited to the differences from the exemplary embodiment in FIG. 2, with reference being made to the description of the exemplary embodiment in FIG. 2 in relation to identical method steps. Method steps that are substantially the same are basically numbered with the same reference numerals.
  • The embodiment of the inventive method shown in FIG. 3 substantially includes the method steps 40, 41, 42 of the first embodiment of the inventive method according to FIG. 2. In addition, the embodiment of the inventive method shown in FIG. 3 has additional method steps and/or substeps. An alternative procedure to that in FIG. 3, which has only some of the additional method steps and/or substeps shown in FIG. 2, is also conceivable. Of course an alternative procedure to that in FIG. 3 can also have additional method steps and/or substeps.
  • The magnetic resonance sequence chosen in further method step 40 can be a steady-state free precession (SSFP) magnetic resonance sequence. However, this is just one possible magnetic resonance sequence for recording the magnetic resonance image data. Other magnetic resonance sequences can of course also be used.
  • The magnetic resonance sequence chosen in further method step 40 has refocusing of a gradient-induced phase development of the spins in the examination region by means of refocusing gradient R. The refocusing gradient R is switched in particular by a refocusing gradient unit of the gradient control module 28. In a further method step 43 parameters of the refocusing gradient R are read out by means of the arithmetic processor 24. These parameters of the refocusing gradient R are passed to the compensation gradient module 33. The compensation gradient module 33 ascertains parameters of the compensation gradient C in further method step 43 as a function of parameters of the refocusing gradient R. The ascertained parameters of the magnetic compensation gradient C can then be set for the compensation gradient C during recording of the magnetic resonance image data in further method step 41.
  • After the positioning of the examination object 15 in the magnetic resonance apparatus 11, adjustment data is in a further method step 44 a by an adjustment data acquisition unit of the magnetic resonance device. For example, a B0 field map is acquired. The field map is acquired in a further method step 44 a before recording of the magnetic resonance image data in further method step 41. The adjustment data is passed from the adjustment data acquisition unit to a parameter adjustment unit. In this way the parameter adjustment unit can ascertain parameters of the magnetic compensation gradient C in a further method step 44 b using the detected B0 field map by the arithmetic processor 24. The ascertained parameters of the magnetic compensation gradient C can then be set for the compensation gradient C during recording of the magnetic resonance image data in a further method step 41. For this purpose, the parameters of the parameter adjustment unit are transmitted to the gradient control module 28 of the magnetic resonance apparatus 11. The gradient control module 28 can then control the gradient coil module 19 using the parameters of the magnetic compensation gradient.
  • In a further method step 41 the compensation gradient C is switched by means of the compensation gradient module 33 during the refocusing gradient R. The compensation gradient C can be switched throughout the entire duration of recording of the magnetic resonance image data. Alternatively, the compensation gradient C can be purposefully switched for refocusing of the spins in the examination region at the end of each repetition interval of the plurality of repetition intervals. The magnetic compensation gradient C is switched in a further method step 41 such that interference, caused by the magnetic interference field, to the refocusing of the spins is at least partially compensated in the examination region.
  • Recording of the magnetic resonance image data in further method step 41 by means of the image data recording module 32 also comprises emitting radio-frequency excitation pulses E with an excitation frequency, with the excitation frequency being chosen such that it matches a resonance frequency of spins in a physical environment of the interference object. In this way, an examination region can be restricted to a vicinity of the interference object by means of the radio-frequency excitation pulses E, which are emitted in particular by means of an excitation pulse unit of the magnetic resonance apparatus 11.
  • The magnetic resonance image data is recorded in a further method step 41, for example by a quantitative magnetic resonance method. In the case shown in FIG. 3 the quantitative magnetic resonance method is a magnetic resonance fingerprinting method. In the further method step 41 a magnetic resonance image is recorded by means of the image data recording module 32 during each repetition interval of the plurality of repetition intervals. The magnetic resonance fingerprinting method includes in particular that recording parameters that have been changed in a pseudo randomized manner are used during recording of the magnetic resonance images.
  • The number of magnetic resonance images recorded in this way are not displayed directly but processed further in a further method step 45 by the arithmetic processor 24. In a first substep 45 a of the further method step 45 a magnetic resonance signal characteristic is generated from the recorded magnetic resonance images. In particular, one signal characteristic is formed by each voxel of the magnetic resonance images over the plurality of magnetic resonance images.
  • In a second substep 45 b of the further method step 45 there is a signal comparison of the generated magnetic resonance signal characteristic with a number of database signal characteristics stored in a database. A database value of at least one tissue parameter is allocated to each database signal characteristic of the number of database signal characteristics. The database is connected in particular in the sense of a data exchange to the arithmetic processor 24. The magnetic resonance signal characteristic is compared by way of example with each of the database signal characteristics. The signal comparison can occur by a conventional pattern recognition method and/or by a correlation analysis. During the signal comparison a comparison parameter is then output for each comparison, and this characterizes the degree of accord between the magnetic resonance signal characteristic and the database signal characteristics.
  • Using the signal comparison a tissue parameter map can be created in this way in a third substep 45 c, and this includes a spatially resolved distribution of the at least one tissue parameter in the examination region. The content of the tissue parameter map is determined by way of example such that an appropriate database signal characteristic of the number of database signal characteristics is ascertained for the magnetic resonance signal characteristic. The appropriate database signal characteristic has in particular the greatest accord with the magnetic resonance signal characteristic. A database value of the at least one tissue parameter linked to the appropriate database signal characteristic can then be included in the tissue parameter map.
  • This method can be repeated for each magnetic resonance signal characteristic of the various voxels of the magnetic resonance images, resulting in a spatially resolved distribution of the at least one tissue parameter. The tissue parameter map can then be output in a further method step 42 on the display unit 25 and/or be stored in the database.
  • The method steps of the inventive method illustrated in FIGS. 2 to 3 are executed by the arithmetic processor 24. For this purpose, the arithmetic processor 24 comprises the required software and/or computer programs which are stored in a memory unit of the arithmetic processor 24. The software and/or computer programs comprise program means which are configured to carry out the inventive method when the computer program and/or the software is run in the arithmetic processor 24 by means of a processor unit of the arithmetic processor 24.
  • FIG. 4 shows a magnetic resonance sequence used in a third embodiment of the inventive method. FIG. 5 shows a magnetic resonance sequence used in a fourth embodiment of the inventive method.
  • The sequences shown in FIG. 4 and FIG. 5 should only be regarded as examples and represent one possibility of how a sequence over time of the magnetic resonance sequence could look. Reference should also be made to the fact that the sequence plans shown in FIG. 4 and FIG. 5 are incomplete since, for example, the spatial encoding gradients and readout windows are not shown. The sequence plans shown in FIG. 4 and FIG. 5 are also illustrated in an abstract manner. This means, only the chronology of sequence elements over time is shown and the exact formation of the sequence elements is not dealt with in detail. In the sequence plans shown in FIG. 4 and FIG. 5 time windows are in each case plotted on different time lines one above the other, in which windows the repetition intervals T, radio-frequency excitation pulses E, refocusing gradient R and compensation gradient C occur. In the sequence plans scaling in the time direction occurs only in arbitrary units for the purpose of simplification.
  • Both sequences as examples have three repetition intervals T1, T2, T3 of the magnetic resonance sequence. Of course, these repetition intervals T1, T2, T3 represent only a section of the magnetic resonance sequence. The magnetic resonance sequence will typically have more repetition intervals T for recording the magnetic resonance image data.
  • Each repetition interval T1, T2, T3 begins with a radio-frequency excitation pulse E1, E2, E3. At the end of each repetition interval T1, T2, T3 there is a refocusing of spins in the examination region by means of refocusing gradient R1, R2, R3.
  • Interference, caused by a magnetic interference field, to the refocusing of the spins in the examination region is at least partially compensated by compensation gradients C1, C2, C3, C′. The compensation gradients C1, C2, C3, C′ are switched during at least part of the duration of recording of the magnetic resonance image data. The compensation gradients C1, C2, C3, C′ are opposed to the magnetic interference field.
  • In the exemplary embodiment shown in FIG. 4 the compensation gradients C1, C2, C3 are switched for refocusing the spins in the examination region at the end of each repetition interval T1, T2, T3. In this way the compensation gradients C1, C2, C3 shown in the exemplary embodiment in FIG. 4 are only switched during the refocusing gradients R1, R2, R3. A first compensation gradient C1 of a first repetition interval Ti therefore occurs during a first refocusing gradient R1 of the first repetition interval T1. A second compensation gradient C2 of a second repetition interval T2 therefore occurs during a second refocusing gradient R2 of the second repetition interval T2. A third compensation gradient C3 of a third repetition interval T3 therefore occurs during a third refocusing gradient R3 of the third repetition interval T3.
  • In the exemplary embodiment shown in FIG. 5 a compensation gradient C′ is switched for the entire duration of recording of the magnetic resonance image data. In this way the compensation gradient C′ according to FIG. 5 is switched not just during the refocusing gradients R1, R2, R3, but also for the remaining duration of the multiple repetition intervals T1, T2, T3.
  • Although modifications and changes may be suggested by those skilled in the art, it is the intention of the inventor to embody within the patent warranted hereon all changes and modifications as reasonably and properly come within the scope of his contribution to the art.

Claims (13)

I claim as my invention:
1. A method for magnetic resonance imaging, comprising:
operating a magnetic resonance scanner to acquire magnetic resonance raw data from an examination region of an examination subject situated in the magnetic resonance scanner, wherein an interference object produces a magnetic interference field in the examination region;
operating said magnetic resonance scanner to acquire said magnetic resonance raw data by executing a magnetic resonance data acquisition sequence comprising a plurality of repetition intervals and refocusing of nuclear spins in the examination region at an end of each repetition interval and comprising, during at least a portion of a duration of acquisition of said magnetic resonance raw data, activation of a magnetic compensation gradient that is opposed to said magnetic interference field; and
compiling said magnetic resonance raw data in a memory and, via a computer, making the compiled magnetic resonance raw data available from said memory as a datafile in electronic form.
2. A method as claimed in claim 1 comprising operating said magnetic resonance scanner in said magnetic resonance data acquisition sequence to activate said magnetic compensation gradient to compensate interference, caused by said magnetic interference field, to the refocusing of the nuclear spins in the examination region.
3. A method as claimed in claim 1 comprising operating said magnetic resonance scanner in said magnetic resonance data acquisition sequence to activate said compensation gradient during an entirety of the duration of acquisition of said magnetic resonance raw data.
4. A method as claimed in claim 1 comprising activating said compensation gradient during the refocusing of the nuclear spins in the examination region at each end of each of repetition interval.
5. A method as claimed in claim 1 comprising refocusing the nuclear spins in the examination region by activating a refocusing gradient that produces a phase development of the nuclear spins in the examination region, and comprising activating said compensation gradient during said refocusing gradient in addition to said refocusing gradient.
6. A method as claimed in claim 5 comprising activating said compensation gradient with compensation gradient parameters that are determined dependent on parameters of said refocusing gradient.
7. A method as claimed in claim 1 comprising operating said magnetic resonance scanner with a steady-state free-precession (SSFP) magnetic resonance sequence as said magnetic resonance data acquisition sequence.
8. A method as claimed in claim 1 comprising operating said magnetic resonance scanner with a quantitative magnetic resonance method embodying said magnetic resonance data acquisition sequence.
9. A method as claimed in claim 8 comprising operating said magnetic resonance scanner with a magnetic resonance fingerprinting method, as said quantitative magnetic resonance method, wherein, during each repetition interval, magnetic resonance raw data for an individual magnetic resonance image are acquired and, in said processor, determining a magnetic resonance signal characteristic from each magnetic resonance image for each respective repetition interval, and making a signal comparison of said signal characteristic with a plurality of database signal characteristics stored in a database that is accessible by said processor, to identify tissue represented in each individual magnetic resonance image as a result of the comparison.
10. A method as claimed in claim 1 comprising operating said magnetic resonance scanner, before acquiring said magnetic resonance raw data, to acquire adjustment data, and setting parameters of said magnetic compensation gradient dependent on said adjustment data.
11. A method as claimed in claim 1 comprising operating said magnetic resonance scanner in said magnetic data acquisition sequence to emit radio-frequency excitation pulses that excite said nuclear spins with an excitation frequency, and selecting said excitation frequency to match a resonance frequency of nuclear spins in a vicinity of said interference object.
12. A magnetic resonance apparatus comprising:
a magnetic resonance scanner;
a control computer configured to operate said magnetic resonance scanner to acquire magnetic resonance raw data from an examination region of an examination subject situated in the magnetic resonance scanner, wherein an interference object produces a magnetic interference field in the examination region;
said control computer being configured to operate said magnetic resonance scanner to acquire said magnetic resonance raw data by executing a magnetic resonance data acquisition sequence comprising a plurality of repetition intervals and refocusing of nuclear spins in the examination region at an end of each repetition interval and comprising, during at least a portion of a duration of acquisition of said magnetic resonance raw data, activation of a magnetic compensation gradient that is opposed to said magnetic interference field; and
said control computer being configured to compile said magnetic resonance raw data in a memory and make the compiled magnetic resonance raw data available from said memory as a datafile in electronic form.
13. A non-transitory, computer-readable data storage medium encoded with programming instructions, said storage medium being loaded into a control computer of a magnetic resonance apparatus that comprises a magnetic resonance scanner, said programming instructions causing said control computer to:
operate said magnetic resonance scanner to acquire magnetic resonance raw data from an examination region of an examination subject situated in the magnetic resonance scanner, wherein an interference object produces a magnetic interference field in the examination region;
operate said magnetic resonance scanner to acquire said magnetic resonance raw data by executing a magnetic resonance data acquisition sequence comprising a plurality of repetition intervals and refocusing of nuclear spins in the examination region at an end of each repetition interval and comprising, during at least a portion of a duration of acquisition of said magnetic resonance raw data, activation of a magnetic compensation gradient that is opposed to said magnetic interference field; and
compile said magnetic resonance raw data in a memory and make the compiled magnetic resonance raw data available from said memory as a datafile in electronic form.
US14/882,793 2014-10-14 2015-10-14 Method and apparatus for magnetic resonance imaging Active 2037-06-14 US10267885B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE102014220776.2A DE102014220776B4 (en) 2014-10-14 2014-10-14 Method for magnetic resonance imaging
DE102014220776 2014-10-14
DE102014220776.2 2014-10-14

Publications (2)

Publication Number Publication Date
US20160103196A1 true US20160103196A1 (en) 2016-04-14
US10267885B2 US10267885B2 (en) 2019-04-23

Family

ID=55644132

Family Applications (1)

Application Number Title Priority Date Filing Date
US14/882,793 Active 2037-06-14 US10267885B2 (en) 2014-10-14 2015-10-14 Method and apparatus for magnetic resonance imaging

Country Status (2)

Country Link
US (1) US10267885B2 (en)
DE (1) DE102014220776B4 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10267885B2 (en) * 2014-10-14 2019-04-23 Siemens Aktiengesellschaft Method and apparatus for magnetic resonance imaging
US11041925B2 (en) 2016-10-06 2021-06-22 Koninklijke Philips N.V. Direct measurement of the B0-off-resonance field during magnetic resonance fingerprinting
US20220229136A1 (en) * 2019-05-10 2022-07-21 Siemens Healthcare Gmbh Magnetic resonance fingerprinting method

Citations (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5154178A (en) * 1990-10-09 1992-10-13 Sri International Method and apparatus for obtaining in-vivo nmr data from a moving subject
US5289127A (en) * 1991-10-25 1994-02-22 The University Of Queensland Correction of signal distortion in an NMR apparatus
US5450010A (en) * 1992-06-29 1995-09-12 U.S. Philips Corporation Magnetic resonance imaging method and apparatus employing eddy current compensation by modification of gradient size
US5455512A (en) * 1992-10-26 1995-10-03 U.S. Philips Corporation Eddy current compensation in magnetic resonance imaging
US5572124A (en) * 1993-12-27 1996-11-05 Hitachi, Ltd. Inspection method and inspection apparatus using nuclear magnetic resonance
US5614827A (en) * 1995-03-30 1997-03-25 Siemens Aktiengesellschaft Method and apparatus for shimming a magnet system of a nuclear magnetic resonance tomography system
US6150815A (en) * 1997-04-10 2000-11-21 The University Of British Columbia Method of correcting for magnetic field inhomogeneity in magnetic resonance imaging
US6737865B2 (en) * 2002-02-22 2004-05-18 Ge Medical Systems Global Technology Company, Llc MRI apparatus
US6842000B2 (en) * 2001-02-28 2005-01-11 Max-Planck-Gesellschaft Zur Forderund Der Wissenschaften E.V. Method and device for acquiring data for diffusion-weighted magnetic resonance imaging
US6891373B2 (en) * 2002-10-31 2005-05-10 Siemens Aktiengesellschaft, Münich Method to determine the ADC coefficients in diffusion-weighted magnetic resonance imaging given use of steady-state sequences
US7034537B2 (en) * 2001-03-14 2006-04-25 Hitachi Medical Corporation MRI apparatus correcting vibratory static magnetic field fluctuations, by utilizing the static magnetic fluctuation itself
US20070052417A1 (en) * 2005-09-02 2007-03-08 Toshiba America Mri, Inc. Method and apparatus for diffusion magnetic resonance imaging with the effects of eddy currents compensated
US7514927B2 (en) * 2005-02-03 2009-04-07 Koninklijke Philips Electronics N.V. MR multi-slice steady state free precession imaging
US20090174404A1 (en) * 2008-01-03 2009-07-09 Allegheny-Singer Research Institute Split-echo with fractional temporal-interpolation
US7567081B2 (en) * 2007-05-03 2009-07-28 University Of Basel Magnetic resonance non-balanced-SSFP method for the detection and imaging of susceptibility related magnetic field distortions
US7683614B2 (en) * 2006-04-27 2010-03-23 Stefan Posse Magnetic resonance spectroscopy with sparse spectral sampling and interleaved dynamic shimming
US20110115487A1 (en) * 2009-11-13 2011-05-19 David Grodzki Method and magnetic resonance system for imaging particles
US8436613B2 (en) * 2009-05-04 2013-05-07 Siemens Aktiengesellschaft Method and magnetic resonance system for diffusion-weighted acquisition of MR signals
US20130197349A1 (en) * 2012-02-01 2013-08-01 Jan Ole BLUMHAGEN Method for calculating a value of an absorption parameter in positron emission tomography
US20140077802A1 (en) * 2012-09-14 2014-03-20 Theresa Bachschmidt Method and control device to control a magnetic resonance system
US8791695B2 (en) * 2009-08-31 2014-07-29 University Of New Brunswick Magnetic resonance apparatus and method
US20140210471A1 (en) * 2013-01-31 2014-07-31 Alto Stemmer Method and control device for operating a magnetic resonance system
US20140225610A1 (en) * 2013-02-12 2014-08-14 Stefan Popescu Magnetic resonance system with pulsed compensation magnetic field gradients
US20140266195A1 (en) * 2013-03-12 2014-09-18 Pavel Levin Method and apparatus for magnetic resonance imaging
US20150268322A1 (en) * 2014-03-18 2015-09-24 Siemens Aktiengesellschaft Method and magnetic resonance apparatus for the acquisition of mr data of a slice within a subject
US20150285878A1 (en) * 2014-04-02 2015-10-08 New York University System, method and computer-accessible medium for spectroscopic localization using simultaneous acquisition of double spin and stimulated echoes
US20150293198A1 (en) * 2014-04-10 2015-10-15 Siemens Aktiengesellschaft Method and apparatus for recording a magnetic resonance data set
US20150362576A1 (en) * 2013-01-25 2015-12-17 Philips Gmbh Metal resistant mr imaging
US20160033602A1 (en) * 2014-07-30 2016-02-04 The Johns Hopkins University Method and apparatus for recording a magnetic resonance dataset of at least one foreign body in a patient
US20160131727A1 (en) * 2014-11-11 2016-05-12 Hyperfine Research, Inc. Pulse sequences for low field magnetic resonance
US9360542B2 (en) * 2012-04-20 2016-06-07 Wisconsin Alumni Research Foundation System and method for spectrally-resolved three-dimensional magnetic resonance imaging without frequency-encoding gradients
US9404987B2 (en) * 2012-04-27 2016-08-02 Siemens Aktiengesellschaft Method for correcting image distortion and system, and magnetic resonance imaging equipment
US20170227621A1 (en) * 2014-08-05 2017-08-10 Hitachi, Ltd. Magnetic resonance imaging apparatus and magnetic resonance imaging method
US20170248672A1 (en) * 2016-02-29 2017-08-31 Siemens Healthcare Gmbh Method and magnetic resonance apparatus for acquiring magnetic resonance dataset with reduced susceptibility artifacts in the reconstruction image

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU1712299A (en) * 1997-12-05 1999-06-28 Pennsylvania State University, The Mri with removal of field inhomogeneity artifacts
US7042220B2 (en) * 2004-04-30 2006-05-09 The Ohio State University Magnetic resonance imaging system and method
WO2006028588A2 (en) * 2004-07-22 2006-03-16 The Regents Of The University Of California Nuclear magnetic resonance detection in inhomogeneous magnetic fields
WO2009020717A1 (en) * 2007-08-09 2009-02-12 Ge Homeland Protection Inc. Method using composite preparation pulse for nqr testing of samples in inhomogenous rf magnetic fields
DE102009033606B4 (en) 2009-07-17 2012-03-08 Siemens Aktiengesellschaft Determination of the strength of a magnetic interference field of a particle
DE102009036237B4 (en) 2009-08-05 2013-10-31 Siemens Aktiengesellschaft Contrast agent-free MR angiography with SSFP sequences
US8723518B2 (en) 2011-03-18 2014-05-13 Nicole SEIBERLICH Nuclear magnetic resonance (NMR) fingerprinting
US10627468B2 (en) 2011-03-18 2020-04-21 Case Western Reserve University Nuclear magnetic resonance (NMR) fingerprinting
DE102014220776B4 (en) * 2014-10-14 2016-06-30 Siemens Healthcare Gmbh Method for magnetic resonance imaging

Patent Citations (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5154178A (en) * 1990-10-09 1992-10-13 Sri International Method and apparatus for obtaining in-vivo nmr data from a moving subject
US5289127A (en) * 1991-10-25 1994-02-22 The University Of Queensland Correction of signal distortion in an NMR apparatus
US5450010A (en) * 1992-06-29 1995-09-12 U.S. Philips Corporation Magnetic resonance imaging method and apparatus employing eddy current compensation by modification of gradient size
US5455512A (en) * 1992-10-26 1995-10-03 U.S. Philips Corporation Eddy current compensation in magnetic resonance imaging
US5572124A (en) * 1993-12-27 1996-11-05 Hitachi, Ltd. Inspection method and inspection apparatus using nuclear magnetic resonance
US5614827A (en) * 1995-03-30 1997-03-25 Siemens Aktiengesellschaft Method and apparatus for shimming a magnet system of a nuclear magnetic resonance tomography system
US6150815A (en) * 1997-04-10 2000-11-21 The University Of British Columbia Method of correcting for magnetic field inhomogeneity in magnetic resonance imaging
US6842000B2 (en) * 2001-02-28 2005-01-11 Max-Planck-Gesellschaft Zur Forderund Der Wissenschaften E.V. Method and device for acquiring data for diffusion-weighted magnetic resonance imaging
US7034537B2 (en) * 2001-03-14 2006-04-25 Hitachi Medical Corporation MRI apparatus correcting vibratory static magnetic field fluctuations, by utilizing the static magnetic fluctuation itself
US6737865B2 (en) * 2002-02-22 2004-05-18 Ge Medical Systems Global Technology Company, Llc MRI apparatus
US6891373B2 (en) * 2002-10-31 2005-05-10 Siemens Aktiengesellschaft, Münich Method to determine the ADC coefficients in diffusion-weighted magnetic resonance imaging given use of steady-state sequences
US7514927B2 (en) * 2005-02-03 2009-04-07 Koninklijke Philips Electronics N.V. MR multi-slice steady state free precession imaging
US20070052417A1 (en) * 2005-09-02 2007-03-08 Toshiba America Mri, Inc. Method and apparatus for diffusion magnetic resonance imaging with the effects of eddy currents compensated
US7218110B2 (en) * 2005-09-02 2007-05-15 Toshiba America Mri, Inc. Method and apparatus for diffusion magnetic resonance imaging with the effects of eddy currents compensated
US7683614B2 (en) * 2006-04-27 2010-03-23 Stefan Posse Magnetic resonance spectroscopy with sparse spectral sampling and interleaved dynamic shimming
US7567081B2 (en) * 2007-05-03 2009-07-28 University Of Basel Magnetic resonance non-balanced-SSFP method for the detection and imaging of susceptibility related magnetic field distortions
US20090174404A1 (en) * 2008-01-03 2009-07-09 Allegheny-Singer Research Institute Split-echo with fractional temporal-interpolation
US7834625B2 (en) * 2008-01-03 2010-11-16 Allegheny-Singer Research Institute Split-echo with fractional temporal-interpolation
US8436613B2 (en) * 2009-05-04 2013-05-07 Siemens Aktiengesellschaft Method and magnetic resonance system for diffusion-weighted acquisition of MR signals
US8791695B2 (en) * 2009-08-31 2014-07-29 University Of New Brunswick Magnetic resonance apparatus and method
US20110115487A1 (en) * 2009-11-13 2011-05-19 David Grodzki Method and magnetic resonance system for imaging particles
US20130197349A1 (en) * 2012-02-01 2013-08-01 Jan Ole BLUMHAGEN Method for calculating a value of an absorption parameter in positron emission tomography
US9220473B2 (en) * 2012-02-01 2015-12-29 Siemens Aktiengesellschaft Method for calculating a value of an absorption parameter in positron emission tomography
US9360542B2 (en) * 2012-04-20 2016-06-07 Wisconsin Alumni Research Foundation System and method for spectrally-resolved three-dimensional magnetic resonance imaging without frequency-encoding gradients
US9404987B2 (en) * 2012-04-27 2016-08-02 Siemens Aktiengesellschaft Method for correcting image distortion and system, and magnetic resonance imaging equipment
US20140077802A1 (en) * 2012-09-14 2014-03-20 Theresa Bachschmidt Method and control device to control a magnetic resonance system
US20150362576A1 (en) * 2013-01-25 2015-12-17 Philips Gmbh Metal resistant mr imaging
US20140210471A1 (en) * 2013-01-31 2014-07-31 Alto Stemmer Method and control device for operating a magnetic resonance system
US20140225610A1 (en) * 2013-02-12 2014-08-14 Stefan Popescu Magnetic resonance system with pulsed compensation magnetic field gradients
US9689952B2 (en) * 2013-02-12 2017-06-27 Siemens Aktiengesellschaft Magnetic resonance system with pulsed compensation magnetic field gradients
US20140266195A1 (en) * 2013-03-12 2014-09-18 Pavel Levin Method and apparatus for magnetic resonance imaging
US9513358B2 (en) * 2013-03-12 2016-12-06 Vaposun Inc. Method and apparatus for magnetic resonance imaging
US20150268322A1 (en) * 2014-03-18 2015-09-24 Siemens Aktiengesellschaft Method and magnetic resonance apparatus for the acquisition of mr data of a slice within a subject
US20150285878A1 (en) * 2014-04-02 2015-10-08 New York University System, method and computer-accessible medium for spectroscopic localization using simultaneous acquisition of double spin and stimulated echoes
US20150293198A1 (en) * 2014-04-10 2015-10-15 Siemens Aktiengesellschaft Method and apparatus for recording a magnetic resonance data set
US10012715B2 (en) * 2014-04-10 2018-07-03 Siemens Aktiengesellschaft Method and apparatus for recording a magnetic resonance data set
US20160033602A1 (en) * 2014-07-30 2016-02-04 The Johns Hopkins University Method and apparatus for recording a magnetic resonance dataset of at least one foreign body in a patient
US20170227621A1 (en) * 2014-08-05 2017-08-10 Hitachi, Ltd. Magnetic resonance imaging apparatus and magnetic resonance imaging method
US20160131727A1 (en) * 2014-11-11 2016-05-12 Hyperfine Research, Inc. Pulse sequences for low field magnetic resonance
US20170248672A1 (en) * 2016-02-29 2017-08-31 Siemens Healthcare Gmbh Method and magnetic resonance apparatus for acquiring magnetic resonance dataset with reduced susceptibility artifacts in the reconstruction image

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Ma et al., Magnetic Resonance Fingerprinting, March 14, 2013. NIH. *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10267885B2 (en) * 2014-10-14 2019-04-23 Siemens Aktiengesellschaft Method and apparatus for magnetic resonance imaging
US11041925B2 (en) 2016-10-06 2021-06-22 Koninklijke Philips N.V. Direct measurement of the B0-off-resonance field during magnetic resonance fingerprinting
US20220229136A1 (en) * 2019-05-10 2022-07-21 Siemens Healthcare Gmbh Magnetic resonance fingerprinting method
US11874355B2 (en) * 2019-05-10 2024-01-16 Siemens Healthcare Gmbh Magnetic resonance fingerprinting method

Also Published As

Publication number Publication date
US10267885B2 (en) 2019-04-23
DE102014220776B4 (en) 2016-06-30
DE102014220776A1 (en) 2016-04-14

Similar Documents

Publication Publication Date Title
US10663545B2 (en) Method and apparatus for low-artifact magnetic resonance fingerprinting scan
US10295635B2 (en) Method and apparatus for acquiring image data from a subject using a magnetic resonance sequence having an adiabatic radio-frequency
US9841476B2 (en) Method and apparatus for magnetic resonance imaging
US10101425B2 (en) Medical imaging apparatus having multiple subsystems, and operating method therefor
US10132900B2 (en) Method and apparatus for magnetic resonance examination of an examination object
US10551467B2 (en) Method and apparatus for movement compensation during magnetic resonance imaging
US10126393B2 (en) Method for magnetic resonance fingerprinting
US10175324B2 (en) Magnetic resonance imaging apparatus and method for control thereof
US10126399B2 (en) Method and apparatus for movement correction in a magnetic resonance fingerprinting examination of a subject
US10261156B2 (en) Method and magnetic resonance apparatus for determining diffusion-weighted image data
CN107440719B (en) Method for displaying quantitative magnetic resonance image data
US20160059041A1 (en) Method and apparatus for monitoring a radiation therapy of a patient
US10451698B2 (en) Method and apparatus for parallel magnetic resonance data acquisition
US10267885B2 (en) Method and apparatus for magnetic resonance imaging
US10254373B2 (en) Method and apparatus for acquiring magnetic resonance data with navigator scans on opposite sides of the examination region
US10031203B2 (en) Method and apparatus for reconstructing image data from undersampled raw magnetic resonance data and reference data
US11747420B2 (en) Actuation of a magnetic resonance device with specific saturation
US10310043B2 (en) Method and apparatus for the correction of magnetic resonance scan data
US10634755B2 (en) Method and apparatus for generating corrected magnetic resonance measurement data
US20150366484A1 (en) Method for determining a spatially resolved distribution of a marker substance
US10151812B2 (en) Magnetic resonance method and apparatus using the same MR signals for determining various parameters
US10401454B2 (en) Method and apparatus assignment of a spin species to a combination image
US10620284B2 (en) Method and apparatus determining a fat content of a liver of a patient using measured spectral magnetic resonance data
US10578698B2 (en) Method and apparatus for acquiring magnetic resonance image data
US20170082709A1 (en) Method and magnetic resonance apparatus for determining dephasing factors in mr multiecho techniques

Legal Events

Date Code Title Description
AS Assignment

Owner name: SIEMENS AKTIENGESELLSCHAFT, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:GRODZKI, DAVID;REEL/FRAME:037801/0153

Effective date: 20151118

STPP Information on status: patent application and granting procedure in general

Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT VERIFIED

STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: SIEMENS HEALTHCARE GMBH, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SIEMENS AKTIENGESELLSCHAFT;REEL/FRAME:049672/0466

Effective date: 20190611

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1551); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 4

AS Assignment

Owner name: SIEMENS HEALTHINEERS AG, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SIEMENS HEALTHCARE GMBH;REEL/FRAME:066088/0256

Effective date: 20231219